This study is NOT currently recruiting participants.
Number
13-D-0014
Sponsoring Institute
National Institute of Dental And Craniofacial Research (NIDCR)
Recruitment Detail
Type: Completed Study; data analyses ongoing Gender: Male & Female Min Age: 18 Max Age: 999
Referral Letter Required
No
Population Exclusion(s)
Children
Keywords
Dental Plaque; Biofilm; Bacterial Interactions; Receptor Polysaccharide; Oral Streptococci; Natural History
Recruitment Keyword(s)
None
Condition(s)
Dental Plaque; Oral Health; Periodontal Disease and Caries; Periodontal Disease
Investigational Drug(s)
Investigational Device(s)
Intervention(s)
Supporting Site
National Institute of Dental and Craniofacial Research
- Dental plaque is a coating of bacteria on the teeth. It contributes to poor dental health and diseases such as gingivitis, cavities and periodontal disease. Researchers who study plaque know that many different types of oral bacteria stick to each other in test-tube experiments. However, it is not clear if these interactions occur in natural dental plaque. By studying how bacteria interact, researchers can better understand how bacteria come together and grow to form plaque.
Objectives:
- To look at how bacteria interact with one another to form dental plaque.
Eligibility:
- Healthy nonsmoking volunteers at least 18 years of age.
Design:
- Participants will be screened with a medical history and dental exam. They will also have dental impressions taken for a stent (a device similar to Invisalign(SqrRoot) braces).
- Participants will wear the stent for up to 8 hours a day on selected study visit days. It will contain enamel chips made from sterilized human teeth. The mouth bacteria will stick to the chips and grow. Chips will be taken out of the stent twice during these study visit days.
- Participants will have other study visits to provide saliva and plaque samples. They will also have gum swabs to collect bacteria.
- Some participants may have a second set of study visits. At these visits, they will chew gum to increase their saliva production. Afterwards, they will wear the stent with the enamel chips for 4 hours. Samples from the stent will be taken once on these study visit days.
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INCLUSION CRITERIA: -Healthy adult subjects (as determined from self-reported medical history, evaluation by study dentist and nursing assessment, per policy). -18 years of age or older -Good oral health as determined by screening oral examination with: --no history of oral cancer -- no active periodontal disease. EXCLUSION CRITERIA: -History of any medical conditions affecting salivary flow, such as Sj(SqrRoot)(Delta)gren s syndrome -History of any immunosuppressant therapy, such as glucocorticoids (within the last year), auto-immune or immune diseases such as ulcerative colitis or systemic lupus erythematosis, or current steroid therapy, other than topical, within the last 30 days -History of cardiac, kidney, liver and lung disorders -Use of tobacco within the last year -Use of antibiotics within the preceding four months -Use of medications thought to affect salivary flow such as head/neck radiation therapy, diuretics, or nitrates. Medications will be checked against product information for effect and reviewed by the protocol dentist. -Clinically visible active dental caries. -Active periodontal disease as defined as no more than 4 sites in the entire mouth with greater than or equal to 5mm probing depths. -History of severe allergic reactions (Anaphylaxis) to several allergins and specific allergies to or other substances found in the stent or impression material (ie: Plasticized Methacrylate Polymer, methyl methacrylate monomer, alkyl dimethacrylate, benzophenone, Toluidine and Hydroquinone), waxes containing Pine Rosin, and to the list of ingredients for the impression material.
-Healthy adult subjects (as determined from self-reported medical history, evaluation by study dentist and nursing assessment, per policy).
-18 years of age or older
-Good oral health as determined by screening oral examination with:
--no history of oral cancer
-- no active periodontal disease.
EXCLUSION CRITERIA:
-History of any medical conditions affecting salivary flow, such as Sj(SqrRoot)(Delta)gren s syndrome
-History of any immunosuppressant therapy, such as glucocorticoids (within the last year), auto-immune or immune diseases such as ulcerative colitis or systemic lupus erythematosis, or current steroid therapy, other than topical, within the last 30 days
-History of cardiac, kidney, liver and lung disorders
-Use of tobacco within the last year
-Use of antibiotics within the preceding four months
-Use of medications thought to affect salivary flow such as head/neck radiation therapy, diuretics, or nitrates. Medications will be checked against product information for effect and reviewed by the protocol dentist.
-Clinically visible active dental caries.
-Active periodontal disease as defined as no more than 4 sites in the entire mouth with greater than or equal to 5mm probing depths.
-History of severe allergic reactions (Anaphylaxis) to several allergins and specific allergies to or other substances found in the stent or impression material (ie: Plasticized Methacrylate Polymer, methyl methacrylate monomer, alkyl dimethacrylate, benzophenone, Toluidine and Hydroquinone), waxes containing Pine Rosin, and to the list of ingredients for the impression material.
Principal Investigator
Referral Contact
For more information: